CN106324116A - Lagotis brachystachya HPLC (high performance liquid chromatography) characteristic spectrum detection method and spectrum thereof - Google Patents
Lagotis brachystachya HPLC (high performance liquid chromatography) characteristic spectrum detection method and spectrum thereof Download PDFInfo
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- CN106324116A CN106324116A CN201510394223.5A CN201510394223A CN106324116A CN 106324116 A CN106324116 A CN 106324116A CN 201510394223 A CN201510394223 A CN 201510394223A CN 106324116 A CN106324116 A CN 106324116A
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Abstract
The invention provides a Lagotis brachystachya HPLC (high performance liquid chromatography) characteristic spectrum detection method and a spectrum thereof. When cascade chromatographic columns are combined for gradient elution, the detection can be completed within 60 minutes. The method has the advantages of high specificity of the obtained characteristic peak, simple and quick operation, low detection cost, favorable reproducibility, high information content and the like, can comprehensively reflect the varieties and quantities of the chemical components contained in the Lagotis brachystachya, and has important meanings for effectively controlling the quality of the Lagotis brachystachya and extract thereof.
Description
Technical field
The present invention relates to HPLC characteristic spectrum detection method and the collection of illustrative plates of a kind of Lagotis brachystachya Maxim., belong to pharmaceutical technology field.
Background technology
Lagotis brachystachya Maxim., Scrophulariaceae Lagos plant, less to its research.Research finds, Lagotis brachystachya Maxim. complicated,
Mainly contain a large amount of Flavonoid substances, and unsatisfactory to its separating effect for the HPLC conventional method of flavonoid detection.
For being difficult to the composition separated, prior art also has the method using Coupled columns, but mostly is cation-exchange chromatography post
Connect with reversed phase chromatographic column, and Coupled columns factor to be considered is a lot: unified general flowing phase, post pressure produce big
Amplitude variation, dead volume sudden change, peak width increase, peak shape is deteriorated and go out peak be difficult to (first outflow first pillar component,
Peak is gone out after causing second pillar reservation reinforcement) etc..Therefore, for Lagotis brachystachya Maxim., needing to set up one simply has
Effect, easy to operate, separation detection effect preferable quality detection method.
Summary of the invention
For the deficiencies in the prior art, the invention provides a kind of Lagotis brachystachya Maxim. HPLC characteristic spectrum detection method and
Collection of illustrative plates.
The present invention, with rutin as object of reference, is followed by phenyl bonded silica post as chromatographic column with octadecylsilane chemically bonded silica post;
With acetonitrile-pH be 6.0 containing volume parts than 0.2% glacial acetic acid, volume parts than the water mixed solution of 0.5% triethylamine be
Flowing phase, by gradient elution, detects Lagotis brachystachya Maxim., and 60min can complete detection, gained HPLC feature
Collection of illustrative plates can more fully reflect kind and the quantity of chemical composition contained by Lagotis brachystachya Maxim..
Technical scheme is as follows:
The HPLC characteristic spectrum detection method of a kind of Lagotis brachystachya Maxim., comprises the steps:
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;With acetonitrile as mobile phase A, with mixed solution that pH is 6.0 as Mobile phase B, by gradient elution, to the short fringe rabbit ear
Grass detects, and its graded is: in flowing mutually, the percentage ratio change of acetonitrile is risen to 20%, 30~60 by 12% in 0~30 minute
Minute risen to 50% by 20%;Detection wavelength is 360nm;Flow velocity: 0.8~1.2ml/min;Number of theoretical plate is calculated by rutin peak
It is not less than 2000;Wherein said Mobile phase B be containing volume parts than 0.2% glacial acetic acid and volume parts than 0.5% triethylamine
Water mixed solution;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.05-0.20mg,
Obtain;
The preparation of need testing solution: take Lagotis brachystachya Maxim. fine powder 10-50mg, adds methanol 10-50ml, supersound process 3-15
Minute, let cool, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and need testing solution each 5~10 μ l respectively, inject high performance liquid chromatograph, record
60-80 minute interior chromatogram, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
Preferably, the HPLC characteristic spectrum detection method of above-mentioned Lagotis brachystachya Maxim., comprise the steps:
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;With acetonitrile as mobile phase A, with mixed solution that pH is 6.0 as Mobile phase B, by gradient elution, to the short fringe rabbit ear
Grass detects, and its graded is: in flowing mutually, the percentage ratio change of acetonitrile is risen to 20%, 30~60 by 12% in 0~30 minute
Minute acetonitrile is risen to 50% by 20%;Detection wavelength is 360nm;Flow velocity: 1.0ml/min;Number of theoretical plate is calculated by rutin peak
It is not less than 2000;Wherein said Mobile phase B be containing volume parts than 0.2% glacial acetic acid and volume parts than 0.5% triethylamine
Water mixed solution;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.1mg, i.e.
?;
The preparation of need testing solution: take Lagotis brachystachya Maxim. fine powder 25mg, adds methanol 25ml, supersound process 5 minutes, puts
Cold, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and need testing solution each 5-10 μ l respectively, inject high performance liquid chromatograph, record 60
Minute interior chromatogram, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
The HPLC characteristic spectrum of above-mentioned Lagotis brachystachya Maxim., including following 10 characteristic peaks, wherein No. 2 peak rutins are reference peak, 10
The relative retention time at individual peak be respectively 0.732 with reference to the ratio of peak retention time, 1.000,1.029,1.080,1.159,1.175,
1.295、1.668、2.561、2.582。
The Lagotis brachystachya Maxim. of the present invention refers to its medical material or extract, and wherein extract refers to through conventional water extract or alcohol extraction
Take thing, or also through compositions that activated carbon or macroporous resin column are the most active constituent-enriched after said extracted.
Weight portion described in this specification is g/ml or kg/l with the unit corresponding relation of parts by volume.
Beneficial effect
The invention provides Lagotis brachystachya Maxim. HPLC characteristic spectrum detection method and collection of illustrative plates, can more fully reflect the short fringe rabbit ear
The kind of the contained chemical composition of grass and quantity, the present invention combines gradient elution by chromatography in series post, and 60min can complete short
The detection of fringe Radix Pecteilis susannae, characteristic peak specificity is strong, have easy and simple to handle, quick, testing cost is low, favorable reproducibility and information
The advantages such as amount is big, have great importance for effectively controlling the quality of Lagotis brachystachya Maxim. and extract thereof.
Accompanying drawing explanation
Fig. 1 is the Lagotis brachystachya Maxim. extractive HPLC characteristic spectrum with octadecylsilane chemically bonded silica post as chromatographic column;
Fig. 2 is to be followed by the octadecylsilane chemically bonded silica post Lagotis brachystachya Maxim. extract as chromatographic column with phenyl bonded silica post
HPLC characteristic spectrum;
Fig. 3 is to be followed by the phenyl bonded silica post Lagotis brachystachya Maxim. extract as chromatographic column with octadecylsilane chemically bonded silica post
HPLC characteristic spectrum;
Fig. 4 is the HPLC characteristic spectrum of Lagotis brachystachya Maxim. extract;
Fig. 5 is the rutin HPLC collection of illustrative plates with reference to product;
The wherein extract that Lagotis brachystachya Maxim. extract is Lagotis brachystachya Maxim. 60% ethanol in Fig. 1-Fig. 4.
Following experimental example and embodiment are used for further illustrating but are not limited to the present invention.
Experimental example 1: chromatographic column contrast choice experiment
Test apparatus: high performance liquid chromatograph: Agilent 1260
Electronic balance: Shimadzu AUW-220D type
Ultraviolet spectrophotometer: Shimadzu UV-2450 type
Reference substance: control substance of Rutin (Nat'l Pharmaceutical & Biological Products Control Institute) lot number: 100080-200707
20150101,20150102 test sample: Lagotis brachystachya Maxim. extract (volumetric concentration 60% ethanol is made by oneself, lot number:,
20150103、20150104、20150201、20150202、20150203、20150204、20150205、20150301)
Chromatographic condition and system suitability: respectively with octadecylsilane chemically bonded silica post, octyl silane group silica gel
Post, phenyl bonded silica post, amino bonded silicagel column and two kinds of Coupled columns detect;With acetonitrile (A)-parts by volume
Number ratio 0.2% glacial acetic acid, volume parts are flowing phase than 0.5% triethylamine aqueous solution (pH is 6.0) (B), gradient elution:
0~30 minute acetonitrile is risen to 20%, 30~60 minute acetonitrile by 12% and is risen to 50% by 20%;Detection wavelength is 360nm;Stream
Speed: 1.0ml/min;Analysis time: 60 minutes.Number of theoretical plate is calculated by rutin should be not less than 2000;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.1mg, i.e.
?;
The preparation of need testing solution: take the finely ground rear fine powder 25mg of Lagotis brachystachya Maxim. extract, adds methanol 25ml, ultrasonic place
Manage 5 minutes, let cool, filter, take subsequent filtrate, to obtain final product.
Detection wavelength: 360nm.
Result: individually with octadecylsilane chemically bonded silica post, octyl silane group silicagel column, phenyl bonded silica post,
Amino bonded silicagel column all can not reach good separating effect, with octadecylsilane chemically bonded silica post as chromatographic column, obtains
7 characteristic peaks, but in the characteristic peak obtained, No. 2 peaks and No. 3 peaks are that two peak overlapping are formed, and specificity is poor, the most not
Selecting octadecylsilane chemically bonded silica post is chromatographic column;And during with two kinds of chromatographic column series windings for chromatographic column, only octadecyl silicon
It is that chromatographic column has relatively good separating effect that alkane bonded silica gel post is followed by phenyl bonded silica post, and remaining serial arrangement all can not
Reach the purpose at separation chromatography peak, and phenyl bonded silica post can only be followed by by octadecylsilane chemically bonded silica post, and phenyl key
Close silicagel column and be followed by octadecylsilane chemically bonded silica post, obtain 8 characteristic peaks, but in the characteristic peak obtained, No. 4 peaks are for many
Individual peak overlapping is formed, and specificity is poor, can not reach separating effect.Therefore, octadecylsilane chemically bonded silica post is selected
Being followed by phenyl bonded silica post is chromatographic column.Wherein Fig. 1-3 is respectively with octadecylsilane chemically bonded silica post, phenyl bonding
Silicagel column is followed by octadecylsilane chemically bonded silica post and octadecylsilane chemically bonded silica post is followed by phenyl bonded silica post and carries out
The chromatogram of detection.
Experimental example 2: the acquisition experiment of Lagotis brachystachya Maxim. HPLC characteristic spectrum
Test apparatus, reference substance, Lagotis brachystachya Maxim. ethanol extraction are with experimental example 1.
Chromatographic condition and system suitability: be followed by phenyl bonded silica post with octadecylsilane chemically bonded silica post and examine
Survey;With acetonitrile (A)-volume parts than 0.2% glacial acetic acid, volume parts than 0.5% triethylamine aqueous solution (pH is for 6.0) (B)
For flowing phase, gradient elution: 0~30 minute acetonitrile is risen to 20%, 30~60 minute acetonitrile by 12% and risen to 50% by 20%;
Detection wavelength is 360nm;Flow velocity: 0.8~1.2ml/min;Analysis time: 60 minutes.Number of theoretical plate is calculated by rutin should not
Less than 2000;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.1mg, i.e.
?;
The preparation of need testing solution: take Lagotis brachystachya Maxim. extract fine powder 25mg, adds methanol 25ml, supersound process 5 points
Clock, lets cool, and filters, takes subsequent filtrate, to obtain final product.
Detection wavelength selects: obtains need testing solution by the preparation method of need testing solution, enters in 190-600nm wave-length coverage
Row scanning, according to ultraviolet absorpting spectrum, selected 360nm is detection wavelength.
Characteristic spectrum obtains: takes 10 batches of Lagotis brachystachya Maxim. extracts and obtains need testing solution by the preparation method of need testing solution,
Obtain the high-efficient liquid phase chromatogram of 10 batches of Lagotis brachystachya Maxim. extracts by above-mentioned chromatographic condition, extract with these 10 batches of Lagotis brachystachya Maxim.s
Based on thing characteristic spectrum, use " similarity evaluation 2004A " to be evaluated, select
The similarity under the 360nm detection wavelength collection of illustrative plates more than 0.9;Result is shown in Fig. 4-Fig. 5.
Experimental example 3: the methodological study experiment of characteristic spectrum detection method
1, precision test
Taking 20150101 batches of Lagotis brachystachya Maxim. extract samples, the test sample obtained by the preparation method of above-mentioned need testing solution is molten
Liquid is a, and under above-mentioned chromatographic condition, continuous sample introduction measures for 5 times, and result shows: the characteristic spectrum detection side that the present invention provides
Method precision is good.Measurement result is shown in Table 1.
Table 1 Lagotis brachystachya Maxim. HPLC characteristic spectrum precision investigates result (relative retention time)
2, replica test
Taking 20150101 batches of Lagotis brachystachya Maxim. extract samples, the test sample obtained by the preparation method of above-mentioned need testing solution is molten
Liquid six parts, under above-mentioned chromatographic condition, sample introduction measures, and result shows: the characteristic spectrum detection method repeatability that the present invention provides
Well.Measurement result is shown in Table 2.
Table 2 Lagotis brachystachya Maxim. HPLC characteristic spectrum repeatability investigates result (relative retention time)
3, stability test
Taking 20150101 batches of Lagotis brachystachya Maxim. extract samples, the test sample obtained by the preparation method of above-mentioned need testing solution is molten
Liquid is a, respectively at 0 hour, 1 hour, 2 hours, 4 hours, 6 hours, 8 hours sample introductions under above-mentioned chromatographic condition
Measuring, result shows: the characteristic spectrum detection method that the present invention provides has good stability.Measurement result is shown in Table 3.
Table 3 Lagotis brachystachya Maxim. HPLC characteristic spectrum study on the stability result (relative retention time)
Following embodiment all can realize the effect described in above-mentioned experimental example.
Detailed description of the invention
Below in conjunction with embodiment, the present invention made detailed elaboration, but be not limited to these embodiments specifically recorded.
Lagotis brachystachya Maxim. 70% ethanol extraction that detected, Lagotis brachystachya Maxim. 50% ethanol extraction, Lagotis brachystachya Maxim. water carry
Take thing, Lagotis brachystachya Maxim. medical material is conventional commercial or self-control.
Embodiment 1: the HPLC characteristic spectrum detection method of Lagotis brachystachya Maxim.
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;With acetonitrile (A)-pH be the volume parts of 6.0 than 0.2% glacial acetic acid, volume parts than 0.5% triethylamine aqueous solution
Mixed solution (B) is flowing phase, gradient elution: 0~30 minute acetonitrile by 12% rise to 20%, 30~60 minute acetonitrile by
20% rises to 50%;Detection wavelength is 360nm;Flow velocity: 1.0ml/min;Number of theoretical plate is calculated by rutin should be not less than 2000;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.1mg, i.e.
?;
The preparation of need testing solution: take Lagotis brachystachya Maxim. 70% ethanol extraction fine powder 10mg, adds methanol 25ml, ultrasonic
Process 5 minutes, let cool, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and each 5 μ l of need testing solution respectively, inject high performance liquid chromatograph, record 60 points
Chromatogram in clock, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
Gained HPLC characteristic spectrum includes 10 characteristic peaks, and wherein No. 2 peak rutins are with reference to peak, when relatively retaining of 10 peaks
Between be respectively 0.731 with the ratio with reference to peak retention time, 1.000,1.028,1.081,1.159,1.177,1.295,1.668,
2.562,2.584, meet above-mentioned standard feature collection of illustrative plates.
Embodiment 2: the HPLC characteristic spectrum detection method of Lagotis brachystachya Maxim.
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;With acetonitrile (A)-pH be the volume parts of 6.0 than 0.2% glacial acetic acid, volume parts than 0.5% triethylamine aqueous solution
Mixed solution (B) is flowing phase, gradient elution: 0~30 minute acetonitrile by 12% rise to 20%, 30~60 minute acetonitrile by
20% rises to 50%;Detection wavelength is 360nm;Flow velocity: 0.8ml/min;Number of theoretical plate is calculated by rutin should be not less than 2000;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.05mg, i.e.
?;
The preparation of need testing solution: take Lagotis brachystachya Maxim. 50% ethanol extraction fine powder 25mg, adds methanol 50ml, ultrasonic
Process 10 minutes, let cool, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and each 10 μ l of need testing solution respectively, inject high performance liquid chromatograph, record 80
Minute interior chromatogram, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
Gained HPLC characteristic spectrum includes 10 characteristic peaks, and wherein No. 2 peak rutins are with reference to peak, when relatively retaining of 10 peaks
Between be respectively 0.733 with the ratio with reference to peak retention time, 1.000,1.031,1.081,1.156,1.175,1.296,1.668,
2.563,2.585, meet above-mentioned standard feature collection of illustrative plates.
Embodiment 3: the HPLC characteristic spectrum detection method of Lagotis brachystachya Maxim.
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;With acetonitrile (A)-pH be the volume parts of 6.0 than 0.2% glacial acetic acid, volume parts than 0.5% triethylamine aqueous solution
Mixed solution (B) is flowing phase, gradient elution: 0~30 minute acetonitrile by 12% rise to 20%, 30~60 minute acetonitrile by
20% rises to 50%;Detection wavelength is 360nm;Flow velocity: 1.2ml/min;Number of theoretical plate is calculated by rutin should be not less than 2000;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.2mg, i.e.
?;
The preparation of need testing solution: take Lagotis brachystachya Maxim. water extract fine powder 20mg, adds methanol 20ml, supersound process 3
Minute, let cool, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and each 5 μ l of need testing solution respectively, inject high performance liquid chromatograph, record 60 points
Chromatogram in clock, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
Gained HPLC characteristic spectrum includes 10 characteristic peaks, and wherein No. 2 peak rutins are with reference to peak, when relatively retaining of 10 peaks
Between be respectively 0.730 with the ratio with reference to peak retention time, 1.000,1.033,1.083,1.153,1.172,1.291,1.668,
2.564,2.588, meet above-mentioned standard feature collection of illustrative plates.
Embodiment 4: the HPLC characteristic spectrum detection method of Lagotis brachystachya Maxim.
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;It is that 6.0 volume parts are than 0.2% glacial acetic acid, volume parts mixing than 0.5% triethylamine aqueous solution with acetonitrile (A)-pH
Close solution (B) for flowing phase, gradient elution: acetonitrile was risen to 20%, 30~60 minute acetonitrile by 20% by 12% in 0~30 minute
Rise to 50%;Detection wavelength is 360nm;Flow velocity: 1.0ml/min;Number of theoretical plate is calculated by rutin should be not less than 2000;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.15mg, i.e.
?;
The preparation of need testing solution: take Lagotis brachystachya Maxim. fine medicinal material powder 25mg, adds methanol 25ml, supersound process 15 minutes,
Let cool, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and each 5 μ l of need testing solution respectively, inject high performance liquid chromatograph, record 60 points
Chromatogram in clock, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
Gained HPLC characteristic spectrum includes 10 characteristic peaks, and wherein No. 2 peak rutins are with reference to peak, when relatively retaining of 10 peaks
Between be respectively 0.732 with the ratio with reference to peak retention time, 1.000,1.031,1.084,1.160,1.174,1.291,1.673,
2.564,2.593, meet above-mentioned standard feature collection of illustrative plates.
Claims (4)
1. a HPLC characteristic spectrum detection method for Lagotis brachystachya Maxim., is characterised by, comprises the steps:
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;With acetonitrile as mobile phase A, with mixed solution that pH is 6.0 as Mobile phase B, by gradient elution, to the short fringe rabbit ear
Grass detects, and its graded is: in flowing mutually, the percentage ratio change of acetonitrile is risen to 20%, 30~60 by 12% in 0~30 minute
Minute risen to 50% by 20%;Detection wavelength is 360nm;Flow velocity: 0.8~1.2ml/min;Number of theoretical plate is calculated by rutin peak
It is not less than 2000;Wherein said Mobile phase B be containing volume parts than 0.2% glacial acetic acid and volume parts than 0.5% triethylamine
Water mixed solution;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.05-0.20mg,
Obtain;
The preparation of need testing solution: take Lagotis brachystachya Maxim. fine powder 10-50mg, adds methanol 10-50ml, supersound process 3-15
Minute, let cool, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and need testing solution each 5~10 μ l respectively, inject high performance liquid chromatograph, record
60-80 minute interior chromatogram, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
The HPLC characteristic spectrum detection method of Lagotis brachystachya Maxim. the most according to claim 1, is characterised by, comprises the steps:
Chromatographic condition and system suitability: be followed by phenyl bonded silica post as chromatograph with octadecylsilane chemically bonded silica post
Post;With acetonitrile as mobile phase A, with mixed solution that pH is 6.0 as Mobile phase B, by gradient elution, to the short fringe rabbit ear
Grass detects, and its graded is: in flowing mutually, the percentage ratio change of acetonitrile is risen to 20%, 30~60 by 12% in 0~30 minute
Minute acetonitrile is risen to 50% by 20%;Detection wavelength is 360nm;Flow velocity: 1.0ml/min;Number of theoretical plate is calculated by rutin peak
It is not less than 2000;Wherein said Mobile phase B be containing volume parts than 0.2% glacial acetic acid and volume parts than 0.5% triethylamine
Water mixed solution;
The preparation of reference substance solution: take control substance of Rutin appropriate, adds methanol and makes every 1ml solution containing rutin 0.1mg, i.e.
?;
The preparation of need testing solution: take Lagotis brachystachya Maxim. fine powder 25mg, adds methanol 25ml, supersound process 5 minutes, puts
Cold, filter, take subsequent filtrate, to obtain final product;
Measure: precision draws reference substance solution and need testing solution each 5-10 μ l respectively, inject high performance liquid chromatograph, record 60
Minute interior chromatogram, obtains the HPLC characteristic spectrum of Lagotis brachystachya Maxim..
3., according to the HPLC characteristic spectrum of the Lagotis brachystachya Maxim. of claim 1 or 2, be characterised by, described in be that Lagotis brachystachya Maxim. refers to
Its medical material or extract, wherein extract refers to through conventional water extract or alcohol extraction thing, or also through making a living after said extracted
Property charcoal or the most active constituent-enriched compositions of macroporous resin column.
The HPLC characteristic spectrum of Lagotis brachystachya Maxim. the most according to claim 1, is characterised by, including following 10 characteristic peaks, its
In No. 2 peak rutins be with reference to peak, the relative retention time at 10 peaks and the ratio with reference to peak retention time is respectively 0.732,1.000,
1.029、1.080、1.159、1.175、1.295、1.668、2.561、2.582。
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Publication number | Priority date | Publication date | Assignee | Title |
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CN112480281A (en) * | 2020-12-12 | 2021-03-12 | 上海容音医疗科技咨询中心 | Leptospermum brachypearia polysaccharide and application thereof in preparing antitumor drugs |
CN112480281B (en) * | 2020-12-12 | 2022-06-10 | 仁合熙德隆药业有限公司 | Leptospermum brachypearia polysaccharide and application thereof in preparing antitumor drugs |
CN114354828A (en) * | 2021-12-29 | 2022-04-15 | 甘肃奇正藏药有限公司 | Leptochloa brachypomum characteristic spectrum, construction method thereof and quality detection method of Leptochloa brachypomum |
CN114354828B (en) * | 2021-12-29 | 2023-11-03 | 甘肃奇正藏药有限公司 | Characteristic spectrum of herba Lagotis Brevibacterium, construction method thereof and quality detection method of herba Lagotis Brevibacterium |
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